Moore CB, Wallace JR, Frase AT, Pendergrass SA, Ritchie MD,
BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge,
BMC Medical Genomics,
05-07-2013,
http://www.biomedcentral.com/1755-8794/6/S2/S6,, Application
[Pubmed ID: 22914216],
Li B, Wang G, Leal SM,
SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits.,
Bioinformatics,
10-15-2012,
https://www.ncbi.nlm.nih.gov/pubmed/?term=22914216,Primary Citation
[Pubmed ID: 25294186],
Wen SH, Yeh JI,
Cohen's h for detection of disease association with rare genetic variants.,
BMC Genomics,
10-08-2014,
https://www.ncbi.nlm.nih.gov/pubmed/?term=25294186,, Application
[Pubmed ID: 27587681],
Lee J, Kim YJ, Lee J, T2D-Genes Consortium., Kim BJ, Lee S, Park T,
Gene-set association tests for next-generation sequencing data.,
Bioinformatics,
09-01-2016,
https://www.ncbi.nlm.nih.gov/pubmed/?term=27587681,, Application
[Pubmed ID: 28039885],
Lee S, Won S, Kim YJ, Kim Y, T2D-Genes Consortium., Kim BJ, Park T,
Rare variant association test with multiple phenotypes.,
Genet Epidemiol,
04-01-2017,
https://www.ncbi.nlm.nih.gov/pubmed/?term=28039885,, Application
[Pubmed ID: 29745849],
Lee S, Kim Y, Choi S, Hwang H, Park T,
Pathway-based approach using hierarchical components of rare variants to analyze multiple phenotypes.,
BMC Bioinformatics,
05-08-2018,
https://www.ncbi.nlm.nih.gov/pubmed/?term=29745849,, Application